Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy1 |
G |
A |
11: 7,111,312 (GRCm39) |
V868I |
probably benign |
Het |
Ahnak |
G |
T |
19: 8,982,269 (GRCm39) |
M1184I |
probably damaging |
Het |
Akap11 |
T |
C |
14: 78,748,928 (GRCm39) |
E1153G |
probably damaging |
Het |
Amy1 |
T |
C |
3: 113,356,376 (GRCm39) |
N260S |
probably null |
Het |
Ankrd6 |
A |
G |
4: 32,824,427 (GRCm39) |
L129P |
probably damaging |
Het |
Aox1 |
A |
T |
1: 58,351,518 (GRCm39) |
T702S |
probably benign |
Het |
Apobec1 |
G |
T |
6: 122,555,845 (GRCm39) |
T204K |
possibly damaging |
Het |
Arhgef19 |
A |
G |
4: 140,976,457 (GRCm39) |
R433G |
probably benign |
Het |
Atf6b |
T |
A |
17: 34,867,618 (GRCm39) |
H110Q |
possibly damaging |
Het |
Btnl4 |
C |
T |
17: 34,694,826 (GRCm39) |
|
probably null |
Het |
Camsap2 |
T |
C |
1: 136,201,521 (GRCm39) |
T662A |
possibly damaging |
Het |
Cbs |
G |
A |
17: 31,843,245 (GRCm39) |
H229Y |
probably damaging |
Het |
Cct8 |
G |
A |
16: 87,287,442 (GRCm39) |
R111* |
probably null |
Het |
Cdc42bpb |
C |
T |
12: 111,293,993 (GRCm39) |
A250T |
probably damaging |
Het |
Chrd |
A |
G |
16: 20,560,097 (GRCm39) |
|
probably benign |
Het |
Ckap2l |
A |
G |
2: 129,117,499 (GRCm39) |
F559L |
probably damaging |
Het |
Cltrn |
A |
G |
X: 162,901,230 (GRCm39) |
D184G |
possibly damaging |
Het |
D630003M21Rik |
T |
C |
2: 158,059,477 (GRCm39) |
Y141C |
probably damaging |
Het |
Dbf4 |
T |
C |
5: 8,447,539 (GRCm39) |
N557S |
probably benign |
Het |
Dct |
T |
G |
14: 118,273,935 (GRCm39) |
N324T |
probably benign |
Het |
Dip2a |
A |
T |
10: 76,114,336 (GRCm39) |
L999* |
probably null |
Het |
Dock10 |
T |
A |
1: 80,520,814 (GRCm39) |
|
probably null |
Het |
Dync2li1 |
A |
T |
17: 84,957,225 (GRCm39) |
D330V |
probably damaging |
Het |
Eif4g3 |
T |
A |
4: 137,907,802 (GRCm39) |
D1267E |
probably benign |
Het |
Enc1 |
A |
G |
13: 97,382,486 (GRCm39) |
E332G |
possibly damaging |
Het |
Fat2 |
C |
T |
11: 55,147,606 (GRCm39) |
V3879I |
probably benign |
Het |
Fh1 |
A |
T |
1: 175,444,114 (GRCm39) |
I117K |
probably damaging |
Het |
Fkbp15 |
A |
G |
4: 62,255,328 (GRCm39) |
L227P |
probably damaging |
Het |
Fpr1 |
T |
A |
17: 18,097,315 (GRCm39) |
M225L |
probably benign |
Het |
Fras1 |
A |
T |
5: 96,918,547 (GRCm39) |
I3528F |
probably damaging |
Het |
Grm7 |
A |
G |
6: 111,184,730 (GRCm39) |
T354A |
probably benign |
Het |
Ift27 |
T |
A |
15: 78,057,978 (GRCm39) |
I9F |
possibly damaging |
Het |
Igf1r |
A |
G |
7: 67,844,729 (GRCm39) |
D834G |
possibly damaging |
Het |
Igsf9b |
T |
A |
9: 27,243,028 (GRCm39) |
L738Q |
probably damaging |
Het |
Itgam |
A |
T |
7: 127,663,904 (GRCm39) |
T44S |
probably benign |
Het |
Ivd |
T |
A |
2: 118,692,515 (GRCm39) |
I5N |
probably benign |
Het |
Jcad |
T |
C |
18: 4,675,780 (GRCm39) |
S1181P |
probably damaging |
Het |
Kctd18 |
A |
G |
1: 57,995,524 (GRCm39) |
V251A |
probably benign |
Het |
Mycbp2 |
A |
G |
14: 103,489,945 (GRCm39) |
V953A |
possibly damaging |
Het |
Myo18a |
T |
C |
11: 77,715,923 (GRCm39) |
|
probably benign |
Het |
Myo3a |
A |
T |
2: 22,345,091 (GRCm39) |
Y509F |
probably damaging |
Het |
Myocd |
C |
A |
11: 65,069,496 (GRCm39) |
M909I |
probably benign |
Het |
Ndufv3 |
G |
A |
17: 31,750,219 (GRCm39) |
R467Q |
probably damaging |
Het |
Nkpd1 |
G |
A |
7: 19,257,177 (GRCm39) |
V319M |
probably damaging |
Het |
Or13p4 |
T |
A |
4: 118,547,389 (GRCm39) |
N87Y |
probably damaging |
Het |
Or1af1 |
T |
C |
2: 37,110,344 (GRCm39) |
V281A |
probably damaging |
Het |
Or1p1c |
C |
T |
11: 74,161,043 (GRCm39) |
A276V |
probably damaging |
Het |
Or2q1 |
G |
T |
6: 42,795,202 (GRCm39) |
A266S |
possibly damaging |
Het |
Or2t1 |
T |
A |
14: 14,328,774 (GRCm38) |
L221Q |
probably damaging |
Het |
Or4c111 |
A |
G |
2: 88,843,722 (GRCm39) |
S229P |
probably benign |
Het |
Or5b101 |
C |
A |
19: 13,005,181 (GRCm39) |
V171L |
probably benign |
Het |
Parp4 |
T |
C |
14: 56,827,329 (GRCm39) |
|
probably benign |
Het |
Pcdhb9 |
A |
G |
18: 37,535,871 (GRCm39) |
T622A |
probably benign |
Het |
Pdpk1 |
A |
T |
17: 24,317,150 (GRCm39) |
|
probably benign |
Het |
Pkhd1 |
C |
A |
1: 20,417,681 (GRCm39) |
G2490V |
probably damaging |
Het |
Plekhg1 |
G |
T |
10: 3,853,658 (GRCm39) |
|
probably null |
Het |
Plekhh2 |
A |
G |
17: 84,882,617 (GRCm39) |
Y708C |
probably damaging |
Het |
Pnp |
T |
C |
14: 51,187,786 (GRCm39) |
F107L |
probably damaging |
Het |
Postn |
T |
A |
3: 54,292,708 (GRCm39) |
|
probably null |
Het |
Prcp |
A |
T |
7: 92,577,883 (GRCm39) |
D349V |
probably damaging |
Het |
Prl3a1 |
A |
T |
13: 27,454,177 (GRCm39) |
I52F |
probably damaging |
Het |
Pym1 |
G |
A |
10: 128,601,913 (GRCm39) |
|
probably benign |
Het |
Rad9a |
A |
T |
19: 4,247,241 (GRCm39) |
I248N |
probably damaging |
Het |
Ror2 |
T |
G |
13: 53,264,341 (GRCm39) |
E917A |
probably benign |
Het |
Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Het |
Sema6d |
A |
G |
2: 124,501,476 (GRCm39) |
|
probably null |
Het |
Shisal1 |
T |
C |
15: 84,290,669 (GRCm39) |
T213A |
probably benign |
Het |
Slc4a2 |
C |
T |
5: 24,632,618 (GRCm39) |
A12V |
probably damaging |
Het |
Slco6b1 |
T |
G |
1: 96,888,901 (GRCm39) |
|
noncoding transcript |
Het |
Slf2 |
A |
T |
19: 44,923,687 (GRCm39) |
H167L |
possibly damaging |
Het |
Snx9 |
G |
T |
17: 5,970,946 (GRCm39) |
G429V |
probably damaging |
Het |
Sod3 |
G |
T |
5: 52,525,504 (GRCm39) |
V68L |
probably benign |
Het |
Spta1 |
T |
A |
1: 174,074,115 (GRCm39) |
D2351E |
probably benign |
Het |
Srpk3 |
G |
A |
X: 72,821,561 (GRCm39) |
R425Q |
possibly damaging |
Het |
Tatdn1 |
C |
T |
15: 58,788,005 (GRCm39) |
G171E |
probably damaging |
Het |
Tbc1d22a |
T |
C |
15: 86,119,770 (GRCm39) |
V22A |
possibly damaging |
Het |
Tnfsf9 |
A |
G |
17: 57,412,738 (GRCm39) |
T103A |
probably benign |
Het |
Tpm3-rs7 |
T |
C |
14: 113,552,595 (GRCm39) |
L163P |
possibly damaging |
Het |
Trim52 |
T |
A |
14: 106,344,401 (GRCm39) |
C20S |
probably damaging |
Het |
Ucp1 |
C |
T |
8: 84,020,661 (GRCm39) |
T157I |
probably damaging |
Het |
Uspl1 |
T |
A |
5: 149,151,224 (GRCm39) |
L794Q |
probably benign |
Het |
Vmn1r5 |
T |
A |
6: 56,962,580 (GRCm39) |
V85E |
probably damaging |
Het |
Vmn2r79 |
A |
G |
7: 86,687,080 (GRCm39) |
I820M |
probably damaging |
Het |
Wscd1 |
C |
A |
11: 71,651,044 (GRCm39) |
P124T |
probably benign |
Het |
Zfp780b |
A |
T |
7: 27,662,525 (GRCm39) |
C677S |
possibly damaging |
Het |
|
Other mutations in Vmn1r58 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01287:Vmn1r58
|
APN |
7 |
5,414,054 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02792:Vmn1r58
|
APN |
7 |
5,414,228 (GRCm39) |
start codon destroyed |
probably null |
0.04 |
IGL03215:Vmn1r58
|
APN |
7 |
5,413,835 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03259:Vmn1r58
|
APN |
7 |
5,414,086 (GRCm39) |
nonsense |
probably null |
|
K7894:Vmn1r58
|
UTSW |
7 |
5,413,702 (GRCm39) |
missense |
probably benign |
0.01 |
R0033:Vmn1r58
|
UTSW |
7 |
5,413,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R0225:Vmn1r58
|
UTSW |
7 |
5,413,865 (GRCm39) |
missense |
probably benign |
0.02 |
R0304:Vmn1r58
|
UTSW |
7 |
5,413,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Vmn1r58
|
UTSW |
7 |
5,413,329 (GRCm39) |
missense |
probably benign |
0.25 |
R0363:Vmn1r58
|
UTSW |
7 |
5,413,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Vmn1r58
|
UTSW |
7 |
5,413,997 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0565:Vmn1r58
|
UTSW |
7 |
5,414,165 (GRCm39) |
missense |
probably benign |
0.06 |
R0612:Vmn1r58
|
UTSW |
7 |
5,413,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Vmn1r58
|
UTSW |
7 |
5,413,676 (GRCm39) |
missense |
probably benign |
0.00 |
R0853:Vmn1r58
|
UTSW |
7 |
5,413,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R0920:Vmn1r58
|
UTSW |
7 |
5,413,788 (GRCm39) |
missense |
probably benign |
0.00 |
R1696:Vmn1r58
|
UTSW |
7 |
5,413,727 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2326:Vmn1r58
|
UTSW |
7 |
5,413,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Vmn1r58
|
UTSW |
7 |
5,413,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R5065:Vmn1r58
|
UTSW |
7 |
5,413,834 (GRCm39) |
missense |
probably benign |
0.00 |
R5087:Vmn1r58
|
UTSW |
7 |
5,413,666 (GRCm39) |
missense |
probably benign |
0.04 |
R5407:Vmn1r58
|
UTSW |
7 |
5,413,872 (GRCm39) |
missense |
probably benign |
0.01 |
R6855:Vmn1r58
|
UTSW |
7 |
5,413,451 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7052:Vmn1r58
|
UTSW |
7 |
5,414,134 (GRCm39) |
missense |
probably benign |
0.04 |
R7334:Vmn1r58
|
UTSW |
7 |
5,414,066 (GRCm39) |
missense |
probably benign |
0.04 |
R7763:Vmn1r58
|
UTSW |
7 |
5,413,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R7840:Vmn1r58
|
UTSW |
7 |
5,414,242 (GRCm39) |
start gained |
probably benign |
|
R7875:Vmn1r58
|
UTSW |
7 |
5,413,753 (GRCm39) |
missense |
probably damaging |
0.98 |
R8004:Vmn1r58
|
UTSW |
7 |
5,413,506 (GRCm39) |
nonsense |
probably null |
|
R8115:Vmn1r58
|
UTSW |
7 |
5,413,341 (GRCm39) |
missense |
probably benign |
0.00 |
R8781:Vmn1r58
|
UTSW |
7 |
5,413,482 (GRCm39) |
missense |
probably benign |
0.00 |
R8802:Vmn1r58
|
UTSW |
7 |
5,414,080 (GRCm39) |
missense |
probably damaging |
1.00 |
X0058:Vmn1r58
|
UTSW |
7 |
5,413,394 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1176:Vmn1r58
|
UTSW |
7 |
5,413,903 (GRCm39) |
missense |
probably damaging |
0.99 |
|